ENST00000322344.8:c.1437G=
MANE Select
|
ENSP00000323511.2:p.Met479=
|
|
ENST00000636840.1:c.59+148G=
|
|
|
ENST00000640501.1:c.43G=
|
|
|
ENST00000322344.7:c.1437G=
|
ENSP00000323511.2:p.Met479=
|
|
ENST00000593946.5:c.*1364G=
|
ENSP00000468896.1:n.*1364G=
|
|
ENST00000594661.5:n.1938G=
|
|
|
ENST00000595081.5:n.340G=
|
|
|
ENST00000596014.5:c.1437G=
|
ENSP00000472300.1:p.Met479=
|
|
ENST00000597965.2:c.144G=
|
ENSP00000471097.2:p.Met48=
|
|
ENST00000599454.5:n.357G=
|
|
|
ENST00000600573.5:c.1344G=
|
ENSP00000469826.1:p.Met448=
|
|
ENST00000600910.5:c.1327G=
|
ENSP00000473137.1:p.Val443=
|
|
ENST00000601816.3:n.509G=
|
|
|
ENST00000625216.2:c.518G=
|
ENSP00000486898.1:n.518G=
|
|
ENST00000627232.2:c.1357G=
|
ENSP00000486037.1:n.1357G=
|
|
ENST00000631020.2:c.1329G=
|
ENSP00000486707.1:p.Met443=
|
|
NM_007254.3:c.1437G=
|
NP_009185.2:p.Met479=
|
|
NM_007254.4:c.1437G=
MANE Select
|
NP_009185.2:p.Met479=
|
|